Avustralya - İngilizce - Department of Health (Therapeutic Goods Administration)

sanofi-aventis australia pty ltd - codeine phosphate hemihydrate, quantity: 30 mg; paracetamol, quantity: 450 mg; doxylamine succinate, quantity: 5 mg - tablet, uncoated - excipient ingredients: sodium starch glycollate; magnesium stearate; purified talc; stearic acid; povidone; pregelatinised maize starch; crospovidone - indications as at 9 june 2020: mersyndol forte is indicated for the short-term management of severe pain for which other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain.

ABD - İngilizce - NLM (National Library of Medicine)

preferred pharmaceuticals, inc. - acetaminophen (unii: 362o9itl9d) (acetaminophen - unii:362o9itl9d), codeine phosphate (unii: gsl05y1mn6) (codeine anhydrous - unii:ux6owy2v7j) - acetaminophen and codeine phosphate tablets are indicated for the management of mild to moderate pain, where treatment with an opioid is appropriate and for which alternative treatments are inadequate. limitations of use because of the risks of addiction, abuse, and misuse, with opioids, even at recommended doses [see warnings ], reserve acetaminophen and codeine phosphate tablets for use in patients for whom alternative treatment options [e.g., non-opioid analgesics] acetaminophen and codeine phosphate tablets are contraindicated for: acetaminophen and codeine phosphate tablets are contraindicated in patients with: acetaminophen and codeine phosphate tablets contain codeine. codeine in combination with acetaminophen, a schedule iii controlled substance. acetaminophen and codeine phosphate tablets contain codeine, a substance with a high potential for abuse similar to other opioids, including fentanyl, hydrocodone, hydromorphone, methadone, morphine, oxycodone, oxymorphone, and tapentadol. acetaminophen and c

Belçika - İngilizce - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

teva b.v. - paracetamol 500 mg; codeine phosphate hemihydrate 30 mg - film-coated tablet - 500 mg - 30 mg - paracetamol 500 mg; codeine phosphate hemihydrate 30 mg - codeine, combinations excl. psycholeptics

Belçika - İngilizce - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

teva b.v. - paracetamol 1000 mg; codeine phosphate hemihydrate 60 mg - film-coated tablet - 1000 mg - 60 mg - paracetamol 1000 mg; codeine phosphate hemihydrate 60 mg - codeine, combinations excl. psycholeptics

Avustralya - İngilizce - Department of Health (Therapeutic Goods Administration)

sandoz pty ltd - codeine phosphate hemihydrate, quantity: 15 mg; paracetamol, quantity: 500 mg - tablet, uncoated - excipient ingredients: colloidal anhydrous silica; povidone; lactose monohydrate; docusate sodium; potato starch; magnesium stearate; ethanol; purified water - for the temporary relief of acute moderate pain in patients over the age of 12 years (see also contraindications and paediatric use)

Avustralya - İngilizce - Department of Health (Therapeutic Goods Administration)

medreich australia pty ltd - codeine phosphate hemihydrate, quantity: 9.6 mg; paracetamol, quantity: 499.9995 mg - tablet, uncoated - excipient ingredients: microcrystalline cellulose; magnesium stearate; quinoline yellow aluminium lake; povidone; croscarmellose sodium; pregelatinised maize starch; maize starch; stearic acid; crospovidone - for the temporary relief of acute moderate pain in patients over the age of 12 years.

Avustralya - İngilizce - Department of Health (Therapeutic Goods Administration)

neo health (otc) pty ltd - codeine phosphate hemihydrate, quantity: 15 mg; paracetamol, quantity: 500 mg - tablet, uncoated - excipient ingredients: methylcellulose; purified talc; calcium stearate; maize starch; povidone - for the temporary relief of acute moderate pain in patients over the age of 18 years

Avustralya - İngilizce - Department of Health (Therapeutic Goods Administration)

neo health (otc) pty ltd - paracetamol, quantity: 500 mg; codeine phosphate hemihydrate, quantity: 8 mg - tablet, uncoated - excipient ingredients: pregelatinised maize starch; povidone; maize starch; magnesium stearate - for the temporary relief of acute moderate pain and fever in patients over the age of 18 years.

Birleşik Krallık - İngilizce - myHealthbox

actavis group ptc ehf - codeine phosphate hemihydrate/paracetamol - film-coated tablets - 30/500mg - codeine, combinations excl. psycholeptics - for the relief of moderate to severe pain in adults and children above 12 years. codeine is indicated in patients older than 12 years of age for the treatment of acute moderate pain which is not considered to be relieved by other analgesics such as paracetamol or ibuprofen (alone).

Birleşik Krallık - İngilizce - myHealthbox

actavis group ptc ehf - codeine phosphate hemihydrate/paracetamol - film-coated tablets - 60/1000mg - codeine, combinations excl. psycholeptics - for the relief of moderate to severe pain in adults and adolescents 16 years and older. codeine is indicated in patients 16 years and older for the treatment of acute moderate pain which is not considered to be relieved by other analgesics such as paracetamol or ibuprofen